State

Iowa product recalls

72,992 recalls have nationwide distribution and so reach Iowa. 5,585 additional recalls listed Iowa specifically in their distribution scope.

What the numbers show

Total: 5,585
Critical: 910
Severe: 1,317
Most recent: 2026-09-16

Of the 5,585 recalls naming Iowa we have scored against our rubric, 910 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,317 (24%) are Severe.

Which agencies issued them

These figures cover only the 5,585 recalls whose distribution notice names Iowa specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8451–8475 of 78577

HighFDA (Food)·F-0368-2025·2025-01-08
Garden Salad with Dressing Recalled Due to Potential Salmonella Contamination
Russ Davis Wholesale is recalling garden salads sold under Crazy Fresh and quick & easy brands due to potential Salmonella contamination in cucumbers. Affected products have sell-by dates of November 6-16, 2024.
Product
Garden Salad w/Ranch Dressing, Net Wt 9oz. Keep Refrigerated. UPC 7 95831-81023 3. Containing Lettuce, tomatoes, cucumbers, cheddar cheese, carrots and hard cooked egg. Sold under the following brands: 1. Crazy Fresh 2. quick & easy, Ready to Enjoy
Category
Food
Distribution
11 states
HighFDA (Devices)·Z-0797-2025·2025-01-08
3M Unitek Orthodontic Primer Recalled Due to Bond Failures and Skin Irritation
3M Unitek is recalling Transbond Plus Self-Etching Primer used in orthodontic bonding due to reports of bracket bond failures and skin irritation or blistering.
Product
3M Unitek Transbond Plus Self-Etching Primer REF 712-090 (100 unit box) 712-091 (20 unit box) Transbond Plus Self Etching Primer is an orthodontic all-in-one etchant and primer that is used in the bonding process of orthodontic appliances to teeth.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0789-2025·2025-01-08
Medline MICRODISECTOMY PACK recalled for endotoxin contamination
Medline custom MICRODISECTOMY PACK kits containing non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination are being recalled. Approximately 1,494 units were distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) MICRODISECTOMY PACK, REF DYNJ80585A; 2) MICRODISECTOMY PACK, REF DYNJ80585B.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V004000·2025-01-08
Blue Bird Recalls 2025 All American Bus for Wiring Defect
Blue Bird is recalling one 2025 All American transit bus because incorrect wiring reverses high and low beams, potentially blinding other drivers.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0771-2025·2025-01-08
Medtronic SynchroMed II and III Implantable Pumps Recalled for Software Defects
Medtronic is recalling SynchroMed II and III implantable pumps used with a clinician tablet app that has software issues in version 2.x. Approximately 319 systems were distributed worldwide.
Product
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900B CLINICIAN TABLET EU -UK with the A810 CP app version 2.x, CFN CT900B
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V003000·2025-01-08
Blue Bird Recalls 2024-2025 All American School Buses for Wiring Defect
Blue Bird is recalling 2024-2025 All American school buses because incorrect wiring reverses high and low beams, potentially blinding other drivers.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-01082025-01·2025-01-08
Chicken Curry Empanadas Recalled For Undeclared Milk Allergen
USDA FSIS issued a public health alert for Chicken Curry Empanadas that may contain undeclared milk. Consumers with milk allergies should not consume these products.
Product
Rajbhog Foods (NJ), Inc. — FSIS Issues Public Health Alert For Chicken Empanada Products Due To Misbranding And Undeclared Allergen
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0320-2025·2025-01-08
Chocolate Raspberry Bakery Products Recalled for Undeclared Allergens and Color Additives
Lithuanian Bakery, Inc. is recalling Chocolate Raspberry baked goods in three sizes due to undeclared milk, soy, peanut, wheat, sulfites, and color dyes. Consumers with allergies should not consume these products.
Product
Chocolate Raspberry: Three sizes, 1. Small, Net Wt 1.25 lbs. (sub ingredients contain, yellow #5 and #6, and red #40 not declared on final product label) 2. Medium, Net Wt 2.75 lbs. (sub ingredients contain milk, yellow #5 and #6, and red #40 not declared on final product labe
Category
Food
Distribution
7 states
HighFDA (Devices)·Z-0772-2025·2025-01-08
SynchroMed II and III implantable pumps recalled for software issues
Medtronic recalled SynchroMed II and III implantable pumps for software issues in the clinician tablet application. Fifty-nine systems are affected.
Product
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900C CLINICIAN TABLET UK with the A810 CP app version 2.x, CFN CT900C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0791-2025·2025-01-08
Medline Deep Brain Stimulation Surgical Kits Recalled for Non-Sterile Contamination
Medline has recalled 128 Deep Brain Stimulation surgical kits for containing non-sterile Surgical Patties and Strips with potential endotoxin contamination. Affected units were distributed worldwide including the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: DEEP BRAIN STIMULATION PACK-LF
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0778-2025·2025-01-08
Medline Surgical Procedure Kits Recalled for Endotoxin Contamination Risk
Medline Industries is recalling 2344 custom surgical kits with non-sterile components that may contain endotoxins. The kits were distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) OPEN HEART CDS-LF, REFCDS840451M; 2) NEURO PACK, REFDYNJ41516M; 3) RFD- AAA PACK, REFDYNJ54242B; 4) OPEN HEART A&B, REFDYNJ901203C; 5) OPEN HEART A&B, REFDYNJ901203D; 6) ACDF-LF, REFDYNJ906681B; 7) ACDF-LF, REFDY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0172-2025·2025-01-08
Dapsone Topical Gel Recalled Due to Crystallization Defect
Viona Pharmaceuticals is recalling Dapsone Gel 7.5% (2760 packs) distributed nationwide due to crystallization in the formulation. The voluntary recall affects lots T400514 and T400808.
Product
DAPSONE — DAPSONE (DAPSONE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0173-2025·2025-01-08
Ketamine injection syringes recalled due to missing tamper-evident seals
Hikma Injectables is recalling 1,800 ketamine injection syringes nationwide because tamper-evident seals are not attached to several syringes, compromising sterility assurance.
Product
ketamine inj 50 mg per 1 mL, Rx Only, 1 mL fill in a 3mL pre-filled syringe, For IV or IM Use, Hikma Injectables USA Inc., 36 Stults Road, Dayton, NJ 08810, This is a Compounded Drug. Hospital/Office Use Only. NDC 63037-137-25
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0779-2025·2025-01-08
Medline Surgical Procedure Kits Recalled for Non-Sterile Components
Medline is recalling custom surgical procedure kits containing non-sterile surgical components with potential endotoxin contamination. The recall affects 1,402 units distributed in the US, Canada, and UAE.
Product
Medline custom medical procedure kits labeled as: 1) VP SHUNT CDS, REF CDS983470D; 2) 1/2X1/2 NEURO SPONGE PACK-LF, REF DYNJ0713177; 3) BURR HOLE SHUNT PACK, REF DYNJ56819D; 4) BURR HOLE SHUNT PACK, REF DYNJ56819F; 5) BURR HOLE SHUNT PACK, REF DYNJ56819G; 6) RO VP SH
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0781-2025·2025-01-08
Medline Nasal Pack Procedure Kits Recalled for Potential Endotoxin Contamination
Medline custom nasal pack procedure kits contain non-sterile surgical components with potential endotoxin contamination. Customers should discontinue use and contact Medline.
Product
Medline custom medical procedure kits labeled as: 1) NASAL PACK, REF DYNJ67789A.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0776-2025·2025-01-08
Baxter Infusion Pump Recalled for Incomplete Post-Repair Testing
Baxter Healthcare is recalling certain infusion pumps that were released after repair without complete testing. Incomplete testing could affect how the device delivers medication to patients.
Product
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8), Product Code 35700BAX2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0775-2025·2025-01-08
Baxter SIGMA Spectrum Infusion Pump Recalled for Incomplete Post-Repair Testing
Baxter is recalling SIGMA Spectrum Infusion Pump (Version 6) units that were released after repair without complete flow testing. The incomplete testing poses a risk of improper device operation.
Product
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), Product Code 35700BAX
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0787-2025·2025-01-08
Medline Surgical Procedure Kits Recalled Due to Sterility Concerns
Medline is recalling custom surgical procedure kits that contain non-sterile surgical supplies with potential for endotoxin contamination. The kits were distributed worldwide, including the United States, United Arab Emirates, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) NEURO BASIN PACK-LF, REF DYNJ39461J; 2) NEURO BASIN KIT, REF DYNJ80200B.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0365-2025·2025-01-08
Sam's Club Hatch Chile Chicken Enchiladas Recalled for Listeria
Sam's Club is recalling Member's Mark Hatch Chile Chicken Enchiladas because the product may contain Listeria monocytogenes.
Product
Member's Mark Hatch Chile Chicken Enchiladas, ready to cook, perishable, packaging type: aluminum/black oven-safe tray Net wt. variable - average 1.52 lbs. UPC 00226529000004, UPC 00409802813793
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0794-2025·2025-01-08
Medline surgical procedure kits recalled for non-sterile components and endotoxin contamination
Medline is recalling 474,300 custom surgical procedure kits because they contain non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination. These components could pose infection risks during surgical procedures.
Product
Medline custom medical procedure kits labeled as: 1) CRANI, REF CDS780089V; 2) CRANIOFACIAL CDS, REF CDS780102K; 3) CRANIOFACIAL CDS, REF CDS780102L; 4) CRANIOFACIAL CDS, REF CDS780102M; 5) CRANIOTOMY CDS-LF, REF CDS780105K; 6) CRANIOTOMY CDS-LF, REF CDS780105L; 7) CRANIO
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0792-2025·2025-01-08
Medline Medical Procedure Kits Recalled for Non-Sterile Component Contamination
Medline Industries is recalling 2,664 custom medical procedure kits containing non-sterile surgical components with potential endotoxin contamination. The affected kits were distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) ENSEMBLE RACHIS-LF, REF DYNJ47568B; 2) UROLOGY ROBOTIC, REF DYNJ55555D; 3) KIT,SPINE LH, REF DYNJ906448A.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0786-2025·2025-01-08
Medline Custom Surgical Kits Recalled for Non-Sterile Components with Endotoxin Risk
Medline Industries is recalling 3,903 custom medical procedure kits due to non-sterile Codman Surgical Patties and Strips with potential for endotoxin contamination. The recall affects products distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) MEM MAXILLOFACIAL PACK-LF, REF DYNJ0660040R; 2) FREE FLAP PACK-LF, REF DYNJ42833A; 3) FREE FLAP PACK-LF, REF DYNJ42833B; 4) TYMPANOPLASTY PACK, REF DYNJ50692C; 5) MAJOR CRANIOTOMY SAFETY, REF DYNJ54736B; 6) FREE FLAP CU
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0774-2025·2025-01-08
SynchroMed II and III Implantable Pumps Recalled for Software Issues
Medtronic has recalled 3,981 SynchroMed implantable pumps worldwide due to software issues in application version 2.x used to program the devices.
Product
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900E CLINICIAN TABLET GLBL SMSNG and PROG CT900E CLINICIAN TABLET PAPER EN with the A810 CP app version 2.x, CFN CT900E
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0773-2025·2025-01-08
Medtronic Implantable Drug Pumps Recalled for Software Defects
Medtronic has recalled 566 SynchroMed II and III implantable drug infusion pumps due to software issues in the controlling application. No injuries or illnesses have been reported.
Product
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900D CLINICIAN TABLET GLOBAL with the A810 CP app version 2.x, CFN CT900D
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0785-2025·2025-01-08
Medline surgical procedure kits recalled for potential endotoxin contamination
Medline is recalling three custom surgical procedure kits due to non-sterile Codman Surgical Patties and Strips that pose a potential endotoxin contamination risk. The affected kits were distributed in the US, Canada, and the UAE.
Product
Medline custom medical procedure kits labeled as: 1) PANENDOSCOPY-LF, REF DYNJ36728C; 2) ENDOSCOPIC SINUS PACK, REF DYNJ40644A; 3) ENDO SINUS PACK, REF DYNJ66449.
Category
Medical Device
Distribution
Distributed nationwide